Evidence map›Paper›PMID 32026099›Full record

ArticleJournal of mammary gland biology and neoplasia2020

The Novel Transcription Factor CREB3L4 Contributes to the Progression of Human Breast Carcinoma.

Qian Pu, Li Lu, Ke Dong, Wen-Wen Geng, Yan-Rong Lv, Hai-Dong Gao

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Journal of mammary gland biology and neoplasia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 26 citations in OpenAlex.

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  12. Transcriptomics analyses reveal the effects of Pentagamaboronon-0-ol on PI3K/Akt and cell cycle of HER2+ breast cancer cells.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Qian PuDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, People's Republic of China.
Li LuDepartment of General Surgery, Shanghai Children's Hospital, Shanghai Jiaotong University, Shanghai, 200040, People's Republic of China.
Ke DongShandong University, Jinan, Shandong, 250012, People's Republic of China.
Wen-Wen GengDepartment of General Surgery, Qilu Hospital (Qingdao) of Shandong University, Qingdao, Shandong, 266035, People's Republic of China.
Yan-Rong LvDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, People's Republic of China. azjlyr@163.com.
Hai-Dong GaoDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, People's Republic of China. haidonggao@sdu.edu.cn.
Shandong University · CNQilu Hospital of Shandong University · CNShanghai Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast carcinoma(BC)is the most common cancer type among females globally. Understanding the molecular pathways that trigger the development of BC is crucial for both prevention and treatment. As such, the role of transcription factors (TFs) in the development of BC is a focal point in this field. CREB3s play a critical role in initiating the unfolded protein response (UPR); however, the role of CREB3 family members in breast cancer development remains largely unknown. Here, we mined the ONCOMINE database for the transcriptional data of CREB3s in patients with BC. Then, the regulatory functions of a novel TF, CREB3L4, were investigated. CREB3L4 knockdown in MDA-MB-231 and MCF-7 cells suppressed proliferation and promoted apoptosis and cell cycle arrest. ChIP assays confirmed that CREB3L4 can directly bind to the PCNA promoter region, suggesting that the PCNA protein may be functionally downstream of CREB3L4. Additionally, the expression level of CREB3L4 was assessed using our cohort. CREB3L4 is upregulated in breast cancer tissues and is significantly associated with histological grade and tumour size (P = 0.001 and P < 0.001, respectively). Furthermore, PCNA expression was upregulated in breast cancer tissues and positively correlated with CREB3L4. In summary, CREB3L4 may play an important role in the progression of human BC and may serve as a therapeutic target.

Indexed as

Gene Expression Regulation, NeoplasticBiomarkers, TumorBreast NeoplasmsCell Cycle CheckpointsCell ProliferationCyclic AMP Response Element-Binding ProteinErb-b2 Receptor Tyrosine KinasesFemaleFollow-Up StudiesHumansMiddle AgedPrognosisReceptors, EstrogenReceptors, ProgesteroneTumor Cells, CulturedBiomarkers, TumorCREB3L4 protein, humanCyclic AMP Response Element-Binding ProteinERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, ProgesteroneBreast carcinomaCREB3L4PCNATranscription factors

Identifiers

PMID32026099
OpenAlexW3005329126

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.